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group_4_presentation_3_-_albinism [2018/11/30 23:01] markovif [Albinism] |
group_4_presentation_3_-_albinism [2018/11/30 23:02] (current) baruaa1 [Symptoms] |
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| ===== Introduction ===== | ===== Introduction ===== | ||
| - | Albinism is characterized as the absence of pigmentation found throughout the body. It is a congenital disorder meaning that it’s effects can be seen from birth, and it can affect both plants as well as animals, ranging from humans to reptiles as an example. In humans, albinism causes changes to the colour of the eyes, skin, and hair, which appear lighter in colour (Albinism, 2018). Some of the symptoms that appear with albinism include a number of vision defects, as well as increased rates of sunburning and skin cancer due to a lack of skin pigmentation (Albinism, 2018). In some rare cases, Albinism may also cause deficiency in immune function and increase the rates of certain infections (Albinism, 2018). | + | Albinism is characterized as the absence of pigmentation found throughout the body. It is a congenital disorder meaning that its effects can be seen from birth, and it can affect both plants as well as animals, ranging from humans to reptiles as an example. In humans, albinism causes changes to the colour of the eyes, skin, and hair, which appear lighter in colour (Albinism, 2018). Some of the symptoms that appear with albinism include a number of vision defects, as well as increased rates of sunburning and skin cancer due to a lack of skin pigmentation (Albinism, 2018). In some rare cases, Albinism may also cause a deficiency in immune function and increase the rates of certain infections (Albinism, 2018). |
| - | Albinism is a recessive genetic disorder and results from inheritance of two alleles containing the mutation. However, due to its recessive nature, the parents of the offspring may or may not be displaying the phenotype while being carriers of the mutated alleles (Albinism, 2018). Albinism occurs due to a mutation that codes for the enzyme tyrosinase, where it is either absent or defective. Tyrosinase is involved in the production of melanin (Albinism, 2018). | + | Albinism is a recessive genetic disorder and results from the inheritance of two alleles containing the mutation. However, due to its recessive nature, the parents of the offspring may or may not be displaying the phenotype while being carriers of the mutated alleles (Albinism, 2018). Albinism occurs due to a mutation that codes for the enzyme tyrosinase, where it is either absent or defective. Tyrosinase is involved in the production of melanin (Albinism, 2018). |
| ===== Epidemiology ===== | ===== Epidemiology ===== | ||
| - | The epidemiology of albinism is still poorly understood, but studies have demonstrated that incidence varies from region to region, and does not preferentially affect one sex over another. In Africa, albinism has an incidence rate of 1 in 4000-5000. In Europe, the incidence rate is roughly 1 in 20,000. In China, the incidence rate is 1 in 18,000. In the United States, the incidence rate is 1 in 16,000. However, incidence rate has been shown to change based on population and genetics, one example is the American Indian Hopi tribe from Arizona which has a much higher incidence rate compared to the rest of the country (1 in 227). Thus, demonstrating that this disease is largely genetic in nature (Kromberg, 2018). | + | The epidemiology of albinism is still poorly understood, but studies have demonstrated that incidence varies from region to region, and does not preferentially affect one sex over another. In Africa, albinism has an incidence rate of 1 in 4000-5000. In Europe, the incidence rate is roughly 1 in 20,000. In China, the incidence rate is 1 in 18,000. In the United States, the incidence rate is 1 in 16,000. However, the incidence rate has been shown to change based on population and genetics, one example is the American Indian Hopi tribe from Arizona which has a much higher incidence rate compared to the rest of the country (1 in 227). Thus, demonstrating that this disease is largely genetic in nature (Kromberg, 2018). |
| The prevalence of types of albinism also vary by ethnic group and location. For example, in the United States, OCA2 is the most common form of albinism and disproportionately affects African Americans and Africans. The estimated frequency is 1 in 10,000 in African-Americans compared with caucasians being 1 in 36,000 (Bashour, 2018). | The prevalence of types of albinism also vary by ethnic group and location. For example, in the United States, OCA2 is the most common form of albinism and disproportionately affects African Americans and Africans. The estimated frequency is 1 in 10,000 in African-Americans compared with caucasians being 1 in 36,000 (Bashour, 2018). | ||
